4.8 Article

A Human Bi-specific Antibody against Zika Virus with High Therapeutic Potential

期刊

CELL
卷 171, 期 1, 页码 229-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2017.09.002

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资金

  1. Singapore Ministry of Education Tier 3 grant [MOE2012-T3-1-008]
  2. National Research Foundation Investigatorship award [NRF-NRFI2016-01]
  3. National Research Foundation Competitive Research Project grant [NRF2016NRF-CRP001-063]
  4. Duke-NUS Signature Research Programme - Ministry of Health, Singapore
  5. US National Institutes of Health [5U19AI109761]
  6. SNF [310030_166445, 157699, KFS-3728-08-2015]
  7. Lions Club Monteceneri
  8. Swiss National Science Foundation (SNF) [310030_166445] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

Zika virus (ZIKV), a mosquito-borne flavivirus, causes devastating congenital birth defects. We isolated a human monoclonal antibody (mAb), ZKA190, that potently cross-neutralizes multi-lineage ZIKV strains. ZKA190 is highly effective in vivo in preventing morbidity and mortality of ZIKV-infected mice. NMR and cryo-electron microscopy show its binding to an exposed epitope on DIII of the E protein. ZKA190 Fab binds all 180 E protein copies, altering the virus quaternary arrangement and surface curvature. However, ZIKV escape mutants emerged in vitro and in vivo in the presence of ZKA190, as well as of other neutralizing mAbs. To counter this problem, we developed a bispecific antibody (FIT-1) comprising ZKA190 and a second mAb specific for DII of E protein. In addition to retaining high in vitro and in vivo potencies, FIT-1 robustly prevented viral escape, warranting its development as a ZIKV immunotherapy.

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